http://identifiers.org/hco/12/GRCh38#113157190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120767061-C-A

113157214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120767036-T-C

113157619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120766458-G-T

113157641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120766436-G-A

113157641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120766436-G-C

113157641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120766436-G-T

113157663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120766414-C-T

113157680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120766397-C-T

http://identifiers.org/hco/12/GRCh38#113157681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120766396-C-A

113157681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120766396-C-T

113157766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766330-G-C

113157766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766330-G-T

113157822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766274-A-G

113157833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766263-G-A

113157833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766263-G-T

113157994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766122-G-C

113157994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766122-G-T

http://identifiers.org/hco/12/GRCh38#113157997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120766119-A-C

113157997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766119-A-G

113158060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766029-G-A

113158060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120766029-G-T

113158086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120765990-T-C

113158129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120765942-A-G

113158149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120765910-A-G

113158149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120765910-A-T

113158382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120765765-G-A

113158382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120765765-G-T

113158485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120765693-G-A

113158485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120765693-G-T

http://identifiers.org/hco/12/GRCh38#113158584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120765614-C-A

113158584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120765614-C-G

113158584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120765614-C-T

http://identifiers.org/hco/12/GRCh38#113158778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120765428-A-C

http://identifiers.org/hco/12/GRCh38#113158832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120765400-C-A

113158849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120765383-A-G

http://identifiers.org/hco/12/GRCh38#113158911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120765321-C-A

113158911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120765321-C-T

113159067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120765165-A-G

113159105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120765127-T-C

113159105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120765127-T-G

113159130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120765100-G-T

113159144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120765087-G-A

113159144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120765087-G-T

113159151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120765080-C-T

http://identifiers.org/hco/12/GRCh38#113161218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120765061-C-A

http://identifiers.org/hco/12/GRCh38#113161257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120765022-C-A

113161257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120765022-C-T

113161432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120764848-G-A

http://identifiers.org/hco/12/GRCh38#113161443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120764837-A-C

113161443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120764837-A-T

http://identifiers.org/hco/12/GRCh38#113161487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120764822-A-C

113161487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120764822-A-G

113161492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120764817-G-A

113161492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120764817-G-C

113161492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120764817-G-T

113161503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, undefined
orthologous variants: 120764806-C-T

113161550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120764764-G-A

113161550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120764764-G-C

113161550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120764764-G-T

http://identifiers.org/hco/12/GRCh38#113161568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120764746-C-A

113161568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120764746-C-T

113161878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120764583-C-G

113161878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120764583-C-T

113162064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120764431-G-C

113162064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120764431-G-T

113162070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120764425-T-A

113162090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120764414-G-T

http://identifiers.org/hco/12/GRCh38#113162927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120764107-C-A

113162927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120764107-C-T

113162965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120764069-T-C

113163083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120763957-G-A

113163083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120763957-G-T

113163191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120763848-C-T

113163200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120763839-C-T

113163344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120763719-C-T

113163712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120763424-G-T

113163713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120763423-A-T

113163925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762996-G-A

113163925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762996-G-T

113163936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762979-G-A

113163936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762979-G-T

http://identifiers.org/hco/12/GRCh38#113163971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120762926-C-A

113163971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762926-C-T

113164004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762876-G-A

113164004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762876-G-T

113164044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762811-G-C

113164044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762811-G-T

http://identifiers.org/hco/12/GRCh38#113164302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120762585-C-A

113164302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762585-C-G

113164302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762585-C-T

http://identifiers.org/hco/12/GRCh38#113164430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120762453-C-A

113164430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120762453-C-G

113165855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense variant
orthologous variants: 120761818-A-T

113165888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense variant
orthologous variants: 120761785-A-G

http://identifiers.org/hco/12/GRCh38#113165933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120761740-A-C

113165933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense variant
orthologous variants: 120761740-A-G

113166029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense variant
orthologous variants: 120761644-A-G

113166030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 120761643-C-T

http://identifiers.org/hco/12/GRCh38#113166075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120761597-C-A

113169680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120761458-G-C

113169680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120761458-G-T

113169760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120761388-C-T

http://identifiers.org/hco/12/GRCh38#113169819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120761329-C-A

113169819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: synonymous variant
orthologous variants: 120761329-C-T

113170043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120761145-G-A

113170043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120761145-G-C

113170043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120761145-G-T

113170047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120761141-G-A

113170047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120761141-G-T

http://identifiers.org/hco/12/GRCh38#113172297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120759957-C-A

113172319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120759935-C-T

http://identifiers.org/hco/12/GRCh38#113172523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120759718-C-A

113172523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense variant
orthologous variants: 120759718-C-T

113172558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: synonymous variant
orthologous variants: 120759683-C-T

113174622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120758840-A-G

113174622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120758840-A-T

113174631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120758831-C-T

113174653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense variant
orthologous variants: 120758808-T-C

113174653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: missense variant
orthologous variants: 120758808-T-G

113174804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120758667-G-A

113174809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120758662-C-T

113174810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120758661-C-G

http://identifiers.org/hco/12/GRCh38#113174816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120758655-C-A

113174816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120758655-C-T

113174866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: intron variant
orthologous variants: 120758605-C-T

113174896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120758575-G-A

113175071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120758407-G-A

113175181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120758297-G-A

113175181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120758297-G-T

113175247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120758230-A-G

113175248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120758229-G-A

113175248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120758229-G-C

113176765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120758017-T-G

http://identifiers.org/hco/12/GRCh38#113176778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120758006-C-A

113176778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120758006-C-T

113176783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120758001-C-G

113176783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120758001-C-T

113176800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120757983-G-A

113176964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120757799-C-T

113176968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120757795-G-T

113176990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120757776-T-C

113176997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120757763-C-T

113177016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120757744-G-A

113177022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120757738-C-T

113177111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120757650-G-A

113177111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120757650-G-T

113177127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120757637-C-G

113177151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120757612-A-G

113177240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120757524-T-A

113177240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120757524-T-G

113177379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120757460-G-A

113177379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120757460-G-T

http://identifiers.org/hco/12/GRCh38#113177429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120757409-A-C

113177481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120757389-T-G

http://identifiers.org/hco/12/GRCh38#113177598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120757284-C-A

http://identifiers.org/hco/12/GRCh38#113178894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120757066-C-A

113178894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120757066-C-T

113178917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120757047-T-C

http://identifiers.org/hco/12/GRCh38#113178957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120757008-A-C

http://identifiers.org/hco/12/GRCh38#113179222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120756772-C-A

113179339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 120756656-G-A

113179393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756623-G-A

113179393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756623-G-T

113179405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756613-T-C

113179671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756483-A-G

http://identifiers.org/hco/12/GRCh38#113179805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120756373-C-A

113179805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756373-C-T

113179826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756353-G-T

113179900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756297-C-T

113179904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756293-G-A

http://identifiers.org/hco/12/GRCh38#113180086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120756139-A-C

113180093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756131-T-A

113180093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756131-T-G

http://identifiers.org/hco/12/GRCh38#113180142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120756092-A-C

113180142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756092-A-G

113180143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120756091-A-G

113180303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120755940-G-A

113180444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120755771-G-C

113180748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120755333-C-T

http://identifiers.org/hco/12/GRCh38#113180763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120755318-C-A

113180988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 120755092-C-T

113180993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120755087-G-A

113181011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120755069-G-C

113181435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120754781-G-A

113181449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120754775-C-T

http://identifiers.org/hco/12/GRCh38#113185168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120751474-C-A

113185168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120751474-C-T

113185194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120751442-C-T

http://identifiers.org/hco/12/GRCh38#113185228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120751406-C-A

113185228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120751406-C-G

113185228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120751406-C-T

113185249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120751396-G-A

113185249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120751396-G-T

http://identifiers.org/hco/12/GRCh38#113185256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#120751389-C-A

113185256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120751389-C-G

113185256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120751389-C-T

113185258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120751387-T-C

113185285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 120751362-G-A

113185285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 120751362-G-C

113185285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 120751362-G-T

113185345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 120751302-G-A

113185345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 120751302-G-T

http://identifiers.org/hco/12/GRCh38#113185358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120751289-C-A

113185358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 120751289-C-G

113185358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 120751289-C-T

113185461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 120751189-G-A

113185461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 120751189-G-C

113185461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 120751189-G-T